A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894085



Internal ID19184939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180638898..180691068hg38UCSC Ensembl
Outerchr4:180638898..180691068hg38UCSC Ensembl
Innerchr4:181560051..181612221hg19UCSC Ensembl
Outerchr4:181560051..181612221hg19UCSC Ensembl
Innerchr4:181797045..181849215hg18UCSC Ensembl
Outerchr4:181797045..181849215hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3852171
hg1952171
hg1852171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781715
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894085
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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